Canonical Allele Identifier: PA302609
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg29578His
CA302606
NM_001267550.2:c.88733G>A